Review
Copyright ©The Author(s) 2016.
World J Cardiol. Feb 26, 2016; 8(2): 163-179
Published online Feb 26, 2016. doi: 10.4330/wjc.v8.i2.163
Table 2 Characteristics of particulate drug delivery systems
CarrierSize range (nm)Preparation methodAdvantages for drug deliveryDisadvantages for drug deliveryRef.
Liposomes and polymerosomes10-2000Self-assembly in aqueous solutionsHigh drug-carrying capacity Good for hydrophobic and hydrophilic drugs Surface functionalization possible Simple preparationBatch-to-batch variability Difficulties in sterilization[123,135,138,141,143,150,161,178]
Microbubbles10-1000Various depending on typeSurface functionalization possibleNot good for hydrophobic drugs Low drug-carrying capacity[145-148,166,168,179]
Polymeric micelles10-100Direct organization or controlled aggregation in solventLong blood circulation time Surface functionalization possible Simple preparationNot good for hydrophobic drugs Low drug-carrying capacity[123,136,137,155,158]
Nanoparticles and nanospheres10-100Nanoparticles: Polymerization of monomers by emulsion Nanospheres: Interfacial polymerization and phase inversion with polymeric emulsionsShape, size and mechanical properties tunable Possibility for controlled releaseToxicity of residual chemicals from preparation process Limited cellular uptake and degradation[123,126,128,139,150,151,155,180]
Dendrimeres1-10Convergent or divergent synthesisHigh functionalized surfaceDifficult preparation process Toxicity[123,154,156]